Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.

Mesenchymal stem cells (MSCs) have the ability to differentiate into a variety of lineages and to renew themselves without malignant changes, and thus hold potential for many clinical applications. However, it has not been well characterized how different the properties of MSCs are depending on the...

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Main Authors: Yusuke Ogata, Yo Mabuchi, Mayu Yoshida, Eriko Grace Suto, Nobuharu Suzuki, Takeshi Muneta, Ichiro Sekiya, Chihiro Akazawa
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4459808?pdf=render
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spelling doaj-eabc525960ea4aa39d532486ef91686a2020-11-24T22:07:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e012909610.1371/journal.pone.0129096Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.Yusuke OgataYo MabuchiMayu YoshidaEriko Grace SutoNobuharu SuzukiTakeshi MunetaIchiro SekiyaChihiro AkazawaMesenchymal stem cells (MSCs) have the ability to differentiate into a variety of lineages and to renew themselves without malignant changes, and thus hold potential for many clinical applications. However, it has not been well characterized how different the properties of MSCs are depending on the tissue source in which they resided. We previously reported a novel technique for the prospective MSC isolation from bone marrow, and revealed that a combination of cell surface markers (LNGFR and THY-1) allows the isolation of highly enriched MSC populations. In this study, we isolated LNGFR(+) THY-1 (+) MSCs from synovium using flow cytometry. The results show that the synovium tissue contained a significantly larger percentage of LNGFR (+) THY-1 (+) MSCs. We examined the colony formation and differentiation abilities of bone marrow-derived MSCs (BM-MSCs) and synovium-derived MSCs (SYN-MSCs) isolated from the same patients. Both types of MSCs exhibited a marked propensity to differentiate into specific lineages. BM-MSCs were preferentially differentiated into bone, while in the SYN-MSC culture, enhanced adipogenic and chondrogenic differentiation was observed. These data suggest that the tissue from which MSCs are isolated should be tailored according to their intended clinical therapeutic application.http://europepmc.org/articles/PMC4459808?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yusuke Ogata
Yo Mabuchi
Mayu Yoshida
Eriko Grace Suto
Nobuharu Suzuki
Takeshi Muneta
Ichiro Sekiya
Chihiro Akazawa
spellingShingle Yusuke Ogata
Yo Mabuchi
Mayu Yoshida
Eriko Grace Suto
Nobuharu Suzuki
Takeshi Muneta
Ichiro Sekiya
Chihiro Akazawa
Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.
PLoS ONE
author_facet Yusuke Ogata
Yo Mabuchi
Mayu Yoshida
Eriko Grace Suto
Nobuharu Suzuki
Takeshi Muneta
Ichiro Sekiya
Chihiro Akazawa
author_sort Yusuke Ogata
title Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.
title_short Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.
title_full Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.
title_fullStr Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.
title_full_unstemmed Purified Human Synovium Mesenchymal Stem Cells as a Good Resource for Cartilage Regeneration.
title_sort purified human synovium mesenchymal stem cells as a good resource for cartilage regeneration.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Mesenchymal stem cells (MSCs) have the ability to differentiate into a variety of lineages and to renew themselves without malignant changes, and thus hold potential for many clinical applications. However, it has not been well characterized how different the properties of MSCs are depending on the tissue source in which they resided. We previously reported a novel technique for the prospective MSC isolation from bone marrow, and revealed that a combination of cell surface markers (LNGFR and THY-1) allows the isolation of highly enriched MSC populations. In this study, we isolated LNGFR(+) THY-1 (+) MSCs from synovium using flow cytometry. The results show that the synovium tissue contained a significantly larger percentage of LNGFR (+) THY-1 (+) MSCs. We examined the colony formation and differentiation abilities of bone marrow-derived MSCs (BM-MSCs) and synovium-derived MSCs (SYN-MSCs) isolated from the same patients. Both types of MSCs exhibited a marked propensity to differentiate into specific lineages. BM-MSCs were preferentially differentiated into bone, while in the SYN-MSC culture, enhanced adipogenic and chondrogenic differentiation was observed. These data suggest that the tissue from which MSCs are isolated should be tailored according to their intended clinical therapeutic application.
url http://europepmc.org/articles/PMC4459808?pdf=render
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